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Hypoxia suppresses myofibroblast differentiation by changing RhoA activity

Research output: Contribution to journalArticle

Original languageEnglish
Article numberjcs223230
Number of pages13
JournalJournal of Cell Science
Volume132
Issue number5
Early online date18 Feb 2019
DOIs
DateAccepted/In press - 9 Jan 2019
DateE-pub ahead of print - 18 Feb 2019
DatePublished (current) - Mar 2019

Abstract

Fibroblasts show a high range of phenotypic plasticity including the transdifferentiating into myofibroblasts. Myofibroblasts are responsible for the generation of the contraction forces that are important for wound healing and scar formation. Overactive myofibroblasts on the other hand are involved in abnormal scarring. Cell stretching and extracellular signals such as transforming growth factor β can induce the myofibroblastic program whereas microenvironmental conditions such as reduced tissue oxygenation have an inhibitory effect. We investigated the effects of hypoxia on myofibroblastic properties and linked this to RhoA activity. Hypoxia reversed the myofibroblastic phenotype of primary fibroblasts. This was accompanied by decreased aSMA expression, alterations in cell contractility, actin reorganization, and RhoA activity. We identified a hypoxia-inducible induction of ArhGAP29, which is critically involved in MRTF-A (myocardin-related transcription factor-A) signaling, the differentiation state of myofibroblasts and modulates RhoA activity. This novel link between hypoxia and MRTF-A signaling is likely to be important for ischemia-induced tissue remodeling and the fibrotic response.

    Research areas

  • hypoxia, ArhGAP29, hypoxia-inducible-factor, myofibroblast, MRTF-A, RhoA

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Documents

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